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dc.contributor.authorZhan, Shuai
dc.contributor.authorMerlin, Christine
dc.contributor.authorBoore, Jeffrey L.
dc.contributor.authorReppert, Steven M.
dc.date2022-08-11T08:09:29.000
dc.date.accessioned2022-08-23T16:32:16Z
dc.date.available2022-08-23T16:32:16Z
dc.date.issued2011-11-23
dc.date.submitted2012-06-21
dc.identifier.citationCell. 2011 Nov 23;147(5):1171-85. <a href="http://dx.doi.org/10.1016/j.cell.2011.09.052">Link to article on publisher's site</a>
dc.identifier.issn0092-8674 (Linking)
dc.identifier.doi10.1016/j.cell.2011.09.052
dc.identifier.pmid22118469
dc.identifier.urihttp://hdl.handle.net/20.500.14038/37845
dc.description.abstractWe present the draft 273 Mb genome of the migratory monarch butterfly (Danaus plexippus) and a set of 16,866 protein-coding genes. Orthology properties suggest that the Lepidoptera are the fastest evolving insect order yet examined. Compared to the silkmoth Bombyx mori, the monarch genome shares prominent similarity in orthology content, microsynteny, and protein family sizes. The monarch genome reveals a vertebrate-like opsin whose existence in insects is widespread; a full repertoire of molecular components for the monarch circadian clockwork; all members of the juvenile hormone biosynthetic pathway whose regulation shows unexpected sexual dimorphism; additional molecular signatures of oriented flight behavior; microRNAs that are differentially expressed between summer and migratory butterflies; monarch-specific expansions of chemoreceptors potentially important for long-distance migration; and a variant of the sodium/potassium pump that underlies a valuable chemical defense mechanism. The monarch genome enhances our ability to better understand the genetic and molecular basis of long-distance migration.
dc.language.isoen_US
dc.relation<a href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=pubmed&cmd=Retrieve&list_uids=22118469&dopt=Abstract">Link to Article in PubMed</a>
dc.relation.urlhttp://dx.doi.org/10.1016/j.cell.2011.09.052
dc.subjectAmino Acid Sequence
dc.subject*Animal Migration
dc.subjectAnimals
dc.subjectBiological Evolution
dc.subjectButterflies
dc.subjectFemale
dc.subjectFlight, Animal
dc.subject*Genome, Insect
dc.subjectInsect Proteins
dc.subjectMale
dc.subject*Molecular Sequence Annotation
dc.subjectMolecular Sequence Data
dc.subjectMoths
dc.subjectNeuropeptides
dc.subjectPhylogeny
dc.subjectSequence Alignment
dc.subjectSmell
dc.subjectNeuroscience and Neurobiology
dc.titleThe monarch butterfly genome yields insights into long-distance migration
dc.typeJournal Article
dc.source.journaltitleCell
dc.source.volume147
dc.source.issue5
dc.identifier.legacycoverpagehttps://escholarship.umassmed.edu/neurobiology_pp/112
dc.identifier.contextkey3013105
html.description.abstract<p>We present the draft 273 Mb genome of the migratory monarch butterfly (Danaus plexippus) and a set of 16,866 protein-coding genes. Orthology properties suggest that the Lepidoptera are the fastest evolving insect order yet examined. Compared to the silkmoth Bombyx mori, the monarch genome shares prominent similarity in orthology content, microsynteny, and protein family sizes. The monarch genome reveals a vertebrate-like opsin whose existence in insects is widespread; a full repertoire of molecular components for the monarch circadian clockwork; all members of the juvenile hormone biosynthetic pathway whose regulation shows unexpected sexual dimorphism; additional molecular signatures of oriented flight behavior; microRNAs that are differentially expressed between summer and migratory butterflies; monarch-specific expansions of chemoreceptors potentially important for long-distance migration; and a variant of the sodium/potassium pump that underlies a valuable chemical defense mechanism. The monarch genome enhances our ability to better understand the genetic and molecular basis of long-distance migration.</p>
dc.identifier.submissionpathneurobiology_pp/112
dc.contributor.departmentReppert Lab
dc.contributor.departmentNeurobiology
dc.source.pages1171-85


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